US2023242644A1PendingUtilityA1

Treatment of metastatic pancreatic adenocarcinoma

Assignee: BIOLINERX LTDPriority: Oct 17, 2018Filed: Feb 14, 2023Published: Aug 3, 2023
Est. expiryOct 17, 2038(~12.3 yrs left)· nominal 20-yr term from priority
A61P 35/04A61P 35/00A61P 1/18A61K 31/4745A61K 31/513A61K 39/3955A61K 38/12C07K 16/2818A61K 45/06A61K 2039/505A61K 2300/00A61K 2039/545A61K 2039/54A61K 38/10A61K 31/519
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Claims

Abstract

A method of treating metastatic pancreatic adenocarcinoma in a subject in need thereof is provided. The method comprising administering to the subject a therapeutically effective amount of each of a peptide set forth in SEQ ID NO: 1, an anti PD-1 and a chemotherapy, thereby treating the metastatic pancreatic adenocarcinoma.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating metastatic pancreatic adenocarcinoma in a subject in need thereof, wherein the subject is post first-line treatment against said metastatic pancreatic adenocarcinoma, the method comprising administering to the subject a therapeutically effective amount of each of a peptide set forth in SEQ ID NO: 1, an anti PD-1 and a chemotherapy, thereby treating the metastatic pancreatic adenocarcinoma. 
     
     
         2 . The method of  claim 1 , wherein said anti PD-1 is pembrolizumab. 
     
     
         3 . The method of  claim 1 , wherein said chemotherapy comprises a plurality of chemotherapeutic agents. 
     
     
         4 . The method of  claim 1 , wherein said chemotherapy comprises irinotecan, fluorouracil (5-FU) and leucovorin (LV). 
     
     
         5 . The method of  claim 4 , wherein said irinotecan is liposome-encapsulated. 
     
     
         6 . The method of  claim 1 , wherein said peptide is administered subcutaneously (SC). 
     
     
         7 . The method of  claim 1 , wherein said peptide is administered at a dose of 1.25 mg/kg. 
     
     
         8 . The method of  claim 1 , wherein said anti PD-1 is administered intravenously (IV). 
     
     
         9 . The method of  claim 1 , wherein said chemotherapy is administered intravenously. 
     
     
         10 . The method of  claim 1 , wherein said treatment comprises a monotherapy period with said peptide followed by a combination therapy with said peptide, said anti PD-1 and said chemotherapy. 
     
     
         11 . The method of  claim 10 , wherein said combination therapy is repeated every 2 weeks with said chemotherapy and every 3 weeks with said anti PD-1. 
     
     
         12 . The method of  claim 10 , wherein said monotherapy is performed on Days 1-5, daily.

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